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Clinical Observation of Clarithromycin Intensive Therapy for Patients with Chronic Rhinosinusitis / 中国药房
China Pharmacy ; (12): 4212-4215, 2017.
Article en Zh | WPRIM | ID: wpr-704410
Biblioteca responsable: WPRO
ABSTRACT
OBJECTIVE:To investigate therapeutic efficacy and safety of clarithromycin intensive therapy on patients with chronic rhinosinusitis and its effects on serum inflammatory cytokines.METHODS:A total of 186 patients with chronic rhinosinusitis were randomly divided into control group 1 (62 cases),control group 2 (62 cases) and observation group (62 cases).Control group 1 was given Amoxicillin and clavulanate potassium tablet (7∶ 1) 0.457 g,3 times a day.Control group 2 was given Clarithromycin dispersible tablet 0.25 g orally,once a day.Observation group was given Clarithromycin dispersible tablet 0.5 g orally on the first week,twice a day,0.25 g at the second week,twice a day.Both groups were treated for 2 weeks.Clinical efficacies of 3 groups were observed.Clinical symptom score,TNF-α,IL-6 and hs-CRP before and after treatment as well as the occurrence of ADR were observed.RESULTS:Total response rate was in descending order:observation group (93.55%) >control group 2 (80.65%) >control group 1 (65.51%),with statistical significance (P<0.05).Before treatment,there was no statistical significance in clinical symptom score,the levels of TNF-α,IL-6 and hs-CRP among 3 groups (P>0.05).After treatment,clinical symptom score,the levels of TNF-αt,IL-6 and hs-CRP were significantly lower than before treatment;those indexes of 3 groups were in ascending order:observation group<control group 2<control group 1,with statistical significance (P<0.05).The incidence of ADR in observation group and control groups were significantly lower than control group 1,with statistical significance (P<0.05).There was no statistical significance between observation group and control group 2 (P>0.05).CONCLUSIONS:Clarithromycin intensive therapy shows significant therapeutic efficacy for chronic rhinosinusitis,improves clinical symptoms of patients and reduces the level of serum inflammatory factor without increasing the occurrence of ADR.
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Texto completo: 1 Índice: WPRIM Idioma: Zh Revista: China Pharmacy Año: 2017 Tipo del documento: Article
Texto completo: 1 Índice: WPRIM Idioma: Zh Revista: China Pharmacy Año: 2017 Tipo del documento: Article